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Showing results (371-380 of 387) with videos related to

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Human Mutation|July 12, 2019
Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variantsMelissa S Cline, Giulia Babbi, Sandra Bonache, et al.
Human Mutation|July 14, 2019
Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variantsLaura Kasak, Constantina Bakolitsa, Zhiqiang Hu, et al.
Genome Medicine|December 20, 2017
Mapping genetic variations to three-dimensional protein structures to enhance variant interpretation: a proposed frameworkGustavo Glusman, Peter W Rose, Andreas Prlić, et al.
Human Mutation|May 26, 2017
Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challengesBinghuang Cai, Biao Li, Nikki Kiga, et al.
The Lancet. Global Health|November 29, 2018
Health disparities across the counties of Kenya and implications for policy makers, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016Tom Achoki, Molly K Miller-Petrie, Scott D Glenn, et al.
Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.
Human Mutation|June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challengesRoxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
BMC Medicine|December 17, 2015
A shortened verbal autopsy instrument for use in routine mortality surveillance systemsPeter Serina, Ian Riley, Andrea Stewart, et al.
BMC Medicine|December 9, 2015
Improving performance of the Tariff Method for assigning causes of death to verbal autopsiesPeter Serina, Ian Riley, Andrea Stewart, et al.
Kidney International|February 27, 2021
Rationale and design of the Kidney Precision Medicine ProjectIan H de Boer, Charles E Alpers, Evren U Azeloglu, et al.
Pageof 39

Showing results (371-380 of 387) with videos related to

Sort By:
Pageof 39
Human Mutation|July 12, 2019
Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variantsMelissa S Cline, Giulia Babbi, Sandra Bonache, et al.
Human Mutation|July 14, 2019
Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variantsLaura Kasak, Constantina Bakolitsa, Zhiqiang Hu, et al.
Genome Medicine|December 20, 2017
Mapping genetic variations to three-dimensional protein structures to enhance variant interpretation: a proposed frameworkGustavo Glusman, Peter W Rose, Andreas Prlić, et al.
Human Mutation|May 26, 2017
Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challengesBinghuang Cai, Biao Li, Nikki Kiga, et al.
The Lancet. Global Health|November 29, 2018
Health disparities across the counties of Kenya and implications for policy makers, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016Tom Achoki, Molly K Miller-Petrie, Scott D Glenn, et al.
Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.
Human Mutation|June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challengesRoxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
BMC Medicine|December 17, 2015
A shortened verbal autopsy instrument for use in routine mortality surveillance systemsPeter Serina, Ian Riley, Andrea Stewart, et al.
BMC Medicine|December 9, 2015
Improving performance of the Tariff Method for assigning causes of death to verbal autopsiesPeter Serina, Ian Riley, Andrea Stewart, et al.
Kidney International|February 27, 2021
Rationale and design of the Kidney Precision Medicine ProjectIan H de Boer, Charles E Alpers, Evren U Azeloglu, et al.
Pageof 39